ClinVar Miner

Submissions for variant NM_004738.5(VAPB):c.-149dup

dbSNP: rs546898989
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000375322 SCV000434552 likely benign Amyotrophic Lateral Sclerosis, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000280776 SCV000434553 likely benign Spinal Muscular Atrophy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001636946 SCV001851657 benign not provided 2019-12-29 criteria provided, single submitter clinical testing

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